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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870933Generated: October 30, 2026

Hydrochloric Acid → 2,3-Diaminobenzoic acid methyl ester

https://huagongshe.com/reaction/1870933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,3-Diaminobenzoic acidHCID 198069—
ReactantSodium BicarbonateHCID 516892—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2,3-Diaminobenzoic acid methyl esterHCID 571825—

Reaction Steps

A solution of 2,3-diaminobenzoic acid (0.2 g, 1.32 mmol) in methanol (40 ml) was saturated with hydrogen chloride as described above, and the mixture was subsequently heated under reflux for 2 hours. The solid residue obtained on evaporation of the solvent was dissolved in water, and the solution was adjusted to pH 7.0 with sodium hydrogen carbonate. After extraction with ethyl acetate (2×30 ml), the combined organic layers were dried (MgSO4), and the solvent was removed to give methyl 2,3-diaminobenzoate as a brown oil which solidified on trituration with petrol (40/60) (121.6 mg, 56%), m.p. 62-63° C. Found: C, 58.35; H, 5.80; N, 16.69. C8H10N2O2 requires C, 57.83; H, 6.02; N, 16.87%; δH (d6 -DMSO), 200 MHz) 3.87 (3H, s, OCH3). 4.90 (2H, br s, Ar-2-NH2), 6.32 (2H, br s, Ar-3-NH2), 6.46-6.54 (1H, t, Ar-5H), 6.80-6.84 (1H, dd, Ar-4H), 7.18-7.23 (1H, dd, Ar-6H); m/z (EI) 166 (M+), 134, 106, 79.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06100283
Source datasetuspto-grants-2000_08
ORD IDord-a30a5ae8b2ec451690d4d381a4092db1
Source noteuspto-grants-2000_08